@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP141829.RAPEg8y4MvzxTrWfTEdaqUenf3XLhSGktlXA0UbCXkkeI
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP141829.RAPEg8y4MvzxTrWfTEdaqUenf3XLhSGktlXA0UbCXkkeI130_head
{
this:
np:hasAssertion
dgn-np:NP141829.RAPEg8y4MvzxTrWfTEdaqUenf3XLhSGktlXA0UbCXkkeI130_assertion
;
np:hasProvenance
dgn-np:NP141829.RAPEg8y4MvzxTrWfTEdaqUenf3XLhSGktlXA0UbCXkkeI130_provenance
;
np:hasPublicationInfo
dgn-np:NP141829.RAPEg8y4MvzxTrWfTEdaqUenf3XLhSGktlXA0UbCXkkeI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP141829.RAPEg8y4MvzxTrWfTEdaqUenf3XLhSGktlXA0UbCXkkeI130_assertion
a
np:Assertion
.
dgn-np:NP141829.RAPEg8y4MvzxTrWfTEdaqUenf3XLhSGktlXA0UbCXkkeI130_provenance
a
np:Provenance
.
dgn-np:NP141829.RAPEg8y4MvzxTrWfTEdaqUenf3XLhSGktlXA0UbCXkkeI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP141829.RAPEg8y4MvzxTrWfTEdaqUenf3XLhSGktlXA0UbCXkkeI130_assertion
{
miriam-gene:2273
a
ncit:C16612
.
lld:C0009081
a
ncit:C7057
.
dgn-gda:DGN9e042fcdb4166bc456355bce8a039a76
sio:SIO_000628
miriam-gene:2273
,
lld:C0009081
;
a
sio:SIO_001122
.
}
dgn-np:NP141829.RAPEg8y4MvzxTrWfTEdaqUenf3XLhSGktlXA0UbCXkkeI130_provenance
{
dgn-np:NP141829.RAPEg8y4MvzxTrWfTEdaqUenf3XLhSGktlXA0UbCXkkeI130_assertion
dcterms:description
"[The results shows that HOXD13 gene mutation was not involved in outbreak in idiopathic congenital talipes equinovarus, but changes of HOXD13 and FHL1 gene expression related to the development of talipes equinovarus malformation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:18244901
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP141829.RAPEg8y4MvzxTrWfTEdaqUenf3XLhSGktlXA0UbCXkkeI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:14+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}